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De-halogen-coupling

Coupling of Alkyl Halides. The Wurtz Reaction De-halogen-coupling... [Pg.449]

Coupling of gem-Dihalides. Pentacarbonyliron effects de-halogenative coupling of dichloro- or dibromodiphenylmethane and benzylic gem-dihalides to form alkenic compounds in good yields (eq 13). ... [Pg.313]

Coupling of Organometallic Compounds with Aryl Halides, Ethers, and Carboxylic Esters Alkyl-de-halogenation. etc. [Pg.661]

Coupling of Aryl Compounds With Arylboronic acid Derivatives Aryl-de-halogenation, and so on Aryl-de-boronylation, and so on... [Pg.899]

The anaerobic degradation of halogenated alkanoic acids has, however, been much less exhaustively examined. Geobacter (Trichlorobacter) thiogenes was able to transform trichloroacetate to dichloroacetate by coupling the oxidation of acetate to CO2 with the reduction of sulfur to sulfide that carries out the dechlorination (De Wever et al. 2000). [Pg.362]

A. Moliton, B. Ratier, and G. Froyer, Etude comparative de jonctions polymeres (PPP) obtenues sur des films ou des pastilles par implantation avec le couple alcalin-halogene, J. Chim. Phys. 86 l) 249 (1989). [Pg.638]

See other pages where De-halogen-coupling is mentioned: [Pg.535]    [Pg.541]    [Pg.568]    [Pg.870]    [Pg.490]    [Pg.665]    [Pg.1450]    [Pg.535]    [Pg.541]    [Pg.568]    [Pg.870]    [Pg.490]    [Pg.665]    [Pg.1450]    [Pg.201]    [Pg.580]    [Pg.268]    [Pg.111]    [Pg.46]    [Pg.396]    [Pg.56]    [Pg.93]    [Pg.583]    [Pg.396]    [Pg.111]    [Pg.524]    [Pg.4382]    [Pg.164]    [Pg.3127]    [Pg.260]    [Pg.700]    [Pg.211]    [Pg.1941]    [Pg.105]    [Pg.369]    [Pg.134]   
See also in sourсe #XX -- [ Pg.449 , Pg.456 , Pg.490 , Pg.665 ]



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De-couple

De-coupling

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